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Search / Trial NCT06304714

Effects of Bothrops Spp. Snake Envenomation on Willebrand Factor Activity in Martinique and French Guiana

Launched by UNIVERSITY HOSPITAL CENTER OF MARTINIQUE · Mar 8, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Snakebite Envenomation French Caribbean (Martinique, French Guiana) Bothrops Species Von Willebrand Factor Endothelial Activity Haemostasis

ClinConnect Summary

This clinical trial is studying how envenomation from different species of Bothrops snakes affects a substance in the blood called Willebrand factor, which plays an important role in blood clotting. The researchers want to understand how the activity of Willebrand factor changes depending on the species of snake that bites a person, particularly in Martinique and French Guiana. By analyzing this, they hope to find out why some snake bites lead to serious bleeding while others cause blood clots or other complications. The ultimate goal is to improve treatment for patients who suffer from snakebites.

To participate in this study, individuals must be at least 18 years old and have been bitten by a confirmed Bothrops snake, experiencing severe symptoms of envenomation. Participants will be admitted to the emergency department and will need to give their consent to take part in the research. Throughout the trial, they can expect to undergo various tests to measure Willebrand factor activity and its effects on their health. It’s important for potential participants to know that this study aims to enhance understanding of snakebite effects, which could lead to more personalized and effective treatments in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Men or Women, at least 18 years old
  • Be admitted to the Emergency Department of the Martinique University Hospital or the Cayenne University Hospital
  • Be the victim of a confirmed Bothrops snake bite in Martinique or French Guyana. The formal identification of the snake by the patient or his entourage is imperative.
  • Have a confirmed diagnosis of stage III envenomation (regional oedema of the limb and/or moderate general symptoms such as moderate hypotension, malaise, vomiting, abdominal pain, diarrhoea) and stage IV (extensive oedema reaching the trunk and/or severe general symptoms such as prolonged hypotension, shock, anaphylactoid reaction, visceral damage)
  • Be able to receive and understand information related to the research
  • Be able to freely give verbal consent to participate in the proposed research
  • Be able to freely give written informed consent to participate in the plasmathèque
  • Be affiliated to the general social security system
  • Exclusion Criteria:
  • Pregnant or breastfeeding woman
  • People who have been treated for snakebite with Bothrops anti-venom Bothrofav® or Antivipmyn-tri®.
  • Known disorders of haemostasis such as haemophilia A (factor VIII deficiency), haemophilia B (factor IX deficiency), vitamin K deficiency, hepato-cellular insufficiency, presence of circulating anticoagulant factors
  • Disseminated intravascular coagulation (DIC)
  • Constitutional and acquired Von Willebrand disease
  • Constitutional and acquired thrombopathies
  • Idiopathic thrombocytopenic purpura
  • Person under legal protection (guardianship, curatorship, safeguard of justice), and person deprived of liberty.

About University Hospital Center Of Martinique

The University Hospital Center of Martinique (CHUM) is a leading healthcare institution dedicated to advancing medical research and improving patient care through innovative clinical trials. As a prominent academic hospital, CHUM integrates cutting-edge research with clinical practice, fostering collaborations among healthcare professionals, researchers, and academic partners. The center is committed to enhancing health outcomes in the Caribbean region by focusing on a diverse range of medical disciplines, ensuring the highest standards of ethical conduct and patient safety in all trials. Through its comprehensive approach, CHUM aims to contribute significantly to medical knowledge and the development of effective treatment options for various health conditions.

Locations

Fort De France, , Martinique

Patients applied

0 patients applied

Trial Officials

REMI NEVIERE, Professor

Study Director

University Hospital of Martinique

DABOR RESIERE, Professor

Principal Investigator

University Hospital of Martinique

HATEM KALLEL, Professor

Principal Investigator

Hospital of Cayenne, FRENCH GUIANA

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported